State
72,940 recalls have nationwide distribution and so reach Wisconsin. 8,408 additional recalls listed Wisconsin specifically in their distribution scope.
Of the 8,408 recalls naming Wisconsin we have scored against our rubric, 1,547 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,957 (23%) are Severe.
Which agencies issued them
These figures cover only the 8,408 recalls whose distribution notice names Wisconsin specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Get Tested International AB is recalling 15 units of its Lactose Intolerance Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 1210 units of its 3 in 1 STI Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 14 units of its Neurotransmitters XL because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 2400 containers of Wecare Calasoothe over current good manufacturing practice deviations.
Philips North America is recalling 2,341 Incisive CT systems because a tube heat exchanger whose screws are not tightened after replacement may detach and damage other components.
Get Tested International AB is recalling 463 units of its Gonorrhea test because the product was distributed without premarket approval or clearance.
Fresenius Kabi USA is recalling 15,862 Ivenix Infusion System large volume pumps because downstream occlusion alarms may occur at low flow rates when a check valve is added to the administration set.
Blossom Pharmaceuticals is recalling 912 containers of Nivagen Zinc Oxide Ointment USP 20%, 15 oz, over current good manufacturing practice deviations.
Get Tested International AB is recalling 1 unit of its Alcohol (ALC) Test Saliva because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 16 units of its Food Intolerance Test Medium because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 5 units of its Food Intolerance Test Small because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 2043 units of its 8 in 1 STI Test Kit because the product was distributed without premarket approval or clearance.
Siemens Medical Solutions USA is recalling 6 MAMMOMAT Inspiration systems because operator tables were sold together with a bus-installation kit they are not released for.
Get Tested International AB is recalling 24 units of its Akkermansia Test because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 33000 containers of Globe Zinc Oxide Ointment USP over current good manufacturing practice deviations.
Blossom Pharmaceuticals is recalling 7,920 bottles of Nivagen Zinc Oxide Ointment USP 20%, 1 oz, over current good manufacturing practice deviations.
Get Tested International AB is recalling 18 units of its Neurotransmitters Basic because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 10 units of its Men's Hormone Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 658 units of its Parasite Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 184 units of its Menopause (FSH) 2 Tests because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 3 units of its Food Sensitivity Test Large because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 8 units of its IBS Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 4 units of its MPOX Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 1 unit of its GI Microbiome Profile Small because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 17 units of its Adrenal Test because the product was distributed without premarket approval or clearance.